Germann R, Hasibeder W, Haisjackl M, Sparr H, Luz G, Pernthaler H, Friesenecker B, Bonatti J, Gruber E, Schwarz B
Department of Anesthesia and General Intensive Care Medicine, University of Innsbruck, Austria.
Crit Care Med. 1995 Sep;23(9):1560-6. doi: 10.1097/00003246-199509000-00017.
To evaluate the effects of dopamine-1-receptor stimulation on intestinal mucosal tissue oxygenation.
Prospective, experimental, controlled trial.
Animal research laboratory.
Anesthetized domestic pigs (30 to 45 kg).
A small segment of the jejunal mucosa and serosa was exposed by midline laparotomy and antimesenteric incision. Fenoldopam, a selective dopamine-1-receptor agonist, was infused in steps, exponentially increasing from 0.6 to 9.6 micrograms/kg/min via a central venous catheter (n = 8, fenoldopam group), whereas a second group (n = 6, saline group) was only given the solvent.
Systemic hemodynamics as well as systemic and jejunal acid base and blood gas variables were measured using an arterial catheter, a thermodilution pulmonary artery catheter, and a jejunal venous catheter. Jejunal mucosal and serosal tissue PO2 were measured by means of Clark-type surface oxygen electrodes. Oxygen saturation and relative concentration of mucosal microvascular hemoglobin were measured by means of tissue reflectance spectrophotometry. In the fenoldopam group, systemic oxygen delivery (12.5 +/- 0.8 mL/kg/min at baseline) increased by 56% (p < .001) above baseline values. Mean arterial pressure remained unchanged. Fenoldopam produced a 51% increase in mucosal PO2 (23.8 +/- 2.8 torr [3.2 +/- 0.4 kPa] at baseline; p < .001) and a 31% increase in mucosal hemoglobin oxygen saturation (55.4 +/- 8.3% at baseline; p < .001), but not change in serosal PO2 (58 +/- 4.8 torr [7.7 +/- 0.6 kPa] at baseline).
Fenoldopam improves tissue oxygenation of the porcine jejunum in a dose-related manner. This effect is limited to the inner mucosal layer. Dopamine-1-receptor agonists should be evaluated in patients presenting with signs of intestinal mucosal ischemia.
评估多巴胺-1-受体刺激对肠黏膜组织氧合的影响。
前瞻性、实验性、对照试验。
动物研究实验室。
麻醉的家猪(30至45千克)。
通过中线剖腹术和系膜对侧切口暴露一小段空肠黏膜和浆膜。通过中心静脉导管逐步输注选择性多巴胺-1-受体激动剂非诺多泮,剂量从0.6微克/千克/分钟呈指数增加至9.6微克/千克/分钟(n = 8,非诺多泮组),而第二组(n = 6,盐水组)仅给予溶剂。
使用动脉导管、热稀释肺动脉导管和空肠静脉导管测量全身血流动力学以及全身和空肠的酸碱及血气变量。通过克拉克型表面氧电极测量空肠黏膜和浆膜组织的PO2。通过组织反射分光光度法测量黏膜微血管血红蛋白的氧饱和度和相对浓度。在非诺多泮组,全身氧输送(基线时为12.5±0.8毫升/千克/分钟)比基线值增加了56%(p <.001)。平均动脉压保持不变。非诺多泮使黏膜PO2增加了51%(基线时为23.8±2.8托[3.2±0.4千帕];p <.001),黏膜血红蛋白氧饱和度增加了31%(基线时为55.4±8.3%;p <.001),但浆膜PO2无变化(基线时为58±4.8托[7.7±0.6千帕])。
非诺多泮以剂量相关的方式改善猪空肠的组织氧合。这种作用仅限于内层黏膜。对于出现肠黏膜缺血迹象的患者,应评估多巴胺-1-受体激动剂。